Source: GWASDB

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs581080
rs581080
TTC39B
9 15305380 intron variant G/C snv 0.72
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement 		0.800 1.000 2 2010 2017
dbSNP: rs581080
rs581080
TTC39B
9 15305380 intron variant G/C snv 0.72
CUI: C0392885
Disease: High density lipoprotein measurement
High density lipoprotein measurement 		0.800 1.000 2 2010 2019
dbSNP: rs471364
rs471364
TTC39B
1.000 0.040 9 15289580 intron variant C/T snv 0.87
CUI: C0392885
Disease: High density lipoprotein measurement
High density lipoprotein measurement 		0.800 1.000 1 2009 2009
dbSNP: rs643531
rs643531
TTC39B
9 15296036 intron variant C/A snv 0.89
CUI: C0392885
Disease: High density lipoprotein measurement
High density lipoprotein measurement 		0.800 1.000 1 2010 2018
dbSNP: rs581080
rs581080
TTC39B
9 15305380 intron variant G/C snv 0.72
CUI: C0428472
Disease: Serum HDL cholesterol measurement
Serum HDL cholesterol measurement 		0.700 1.000 2 2010 2013
dbSNP: rs471364
rs471364
TTC39B
1.000 0.040 9 15289580 intron variant C/T snv 0.87
CUI: C0428472
Disease: Serum HDL cholesterol measurement
Serum HDL cholesterol measurement 		0.700 1.000 1 2009 2009
dbSNP: rs471364
rs471364
TTC39B
1.000 0.040 9 15289580 intron variant C/T snv 0.87
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease 		0.700 1.000 1 2011 2011
dbSNP: rs643531
rs643531
TTC39B
9 15296036 intron variant C/A snv 0.89
CUI: C0428472
Disease: Serum HDL cholesterol measurement
Serum HDL cholesterol measurement 		0.700 1.000 1 2010 2010
dbSNP: rs6474902
rs6474902
TTC39B
9 15293948 intron variant C/G;T snv
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.700 1.000 1 2012 2012